Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10132085	1.00[EUR][1000 genomes]
rs10132376	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10138731	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10141923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10873318	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12100534	0.88[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12100535	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12323467	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12431997	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12435491	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12435510	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12436134	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12437077	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2370825	1.00[EUR][1000 genomes]
rs28538310	1.00[EUR][1000 genomes]
rs28599647	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35834627	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60650553	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7160080	0.87[EUR][1000 genomes]
rs8018626	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79033000-79038600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:79033800-79034800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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